Original Investigation
May 12, 2025
Antihypertensive Medication Timing and Cardiovascular Events and Death: The BedMed Randomized Clinical Trial
Scott R. Garrison, Jeffrey A. Bakal, Michael R. Kolber, et al
JAMA. Published online May 12, 2025. doi:10.1001/jama.2025.4390
Question Does bedtime administration of blood pressure–lowering medication, compared with conventional morning use, reduce a composite of death or major cardiovascular events?
Findings In this randomized trial of 3357 Canadian primary care patients with hypertension followed up for a median of 4.6 years, bedtime administration of antihypertensive medications had no effect on death or major cardiovascular events (2.3 per 100 patient-years vs 2.4 per 100 patient-years with morning antihypertensive use; adjusted hazard ratio, 0.96). There was no difference in visual, cognitive, or fall- and/or fracture-related safety outcomes.
Meaning Among adults with hypertension in primary care, bedtime administration of antihypertensive medications was safe but did not reduce cardiovascular risk.
Abstract
Importance Whether administration of blood pressure medications at bedtime instead of in the morning reduces cardiovascular risk is unknown, as findings from large clinical trials have not been consistent. There is also concern that bedtime antihypertensive use could induce glaucoma-related visual loss or other hypotensive/ischemic adverse effects.
Objective To determine the effect of bedtime vs morning administration of antihypertensive medications on major cardiovascular events and death.
Design, Setting, and Participants Multicenter, open-label, pragmatic randomized clinical trial with blinded end-point assessment and recruitment via 436 primary care clinicians across 5 Canadian provinces inviting their community-dwelling adult patients with hypertension taking at least 1 once-daily antihypertensive medication. Participants were recruited from March 31, 2017, to May 26, 2022, with final follow-up on December 22, 2023.
Interventions Participants were randomized in a 1:1 ratio to using all once-daily antihypertensive medications either at bedtime (intervention group; n = 1677) or in the morning (control group; n = 1680).
Main Outcomes and Measures The primary outcome was time to first occurrence of all-cause death or hospitalization/emergency department (ED) visit for stroke, acute coronary syndrome, or heart failure. All-cause unplanned hospitalizations/ED visits, and visual, cognitive, and fall- and/or fracture-related safety outcomes were also assessed.
Results A total of 3357 adults (56.4% female; median age, 67 years; 53.7% taking monotherapy) were randomized and followed up for a median of 4.6 years in each treatment group. The composite primary outcome event occurred at a rate of 2.3 per 100 patient-years in the bedtime group and 2.4 per 100 patient-years in the morning group (adjusted hazard ratio, 0.96; 95% CI, 0.77-1.19; P = .70). Individual components of the primary outcome, all-cause hospitalizations/ED visits, and safety outcomes did not differ between groups. In particular, there was no difference in falls or fractures, new glaucoma diagnoses, or 18-month cognitive decline.
Conclusions and Relevance Among adults with hypertension in primary care, bedtime administration of antihypertensive medications was safe but did not reduce cardiovascular risk. Antihypertensive medication administration time did not affect the risks and benefits of blood pressure–lowering medication and instead should be guided by patient preferences.
Trial Registration ClinicalTrials.gov Identifier: NCT02990663
